Letter to the editor regarding “association between sarcopenia on residual back pain after percutaneous kyphoplasty for osteoporotic vertebral compression fractures”

We commend Chengming Li et al. for examining the link between sarcopenia and residual back pain after PKP. However, their retrospective single‑center study (N = 231) has notable limitations. Sarcopenia was diagnosed solely via SMI at T12 on CT, without functional measures (e.g., grip strength, gait speed), and T12 is not a standard spinal muscle evaluation level, risking diagnostic bias. Pain was assessed only by VAS, lacking detail on characteristics or frequency, hindering mechanistic insight. Causal inference is weak due to unaddressed reverse causality-pre‑operative pain may cause disuse atrophy-and uncontrolled confounders like protein intake, vitamin D, and medications. Methodological transparency is insufficient: missing data handling among 472 initial patients was unspecified, and surgical details (team, experience, cement distribution) were omitted, affecting reproducibility. Finally, proposed mechanisms (biomechanical imbalance, chronic inflammation) rely solely on cited literature without direct validation from study data, such as inflammatory markers or spinal stability assessments.

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Publication Details

Journal
Journal of Orthopaedic Surgery and Research
Published
2026-03-24
DOI
https://doi.org/10.1186/s13018-025-06648-5
Primary Topic
Bone health and osteoporosis research
Type
article
Field-Weighted Citation Impact
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article

Letter to the editor regarding “association between sarcopenia on residual back pain after percutaneous kyphoplasty for osteoporotic vertebral compression fractures”

Journal of Orthopaedic Surgery and Research
Bone health and osteoporosis research
article

Letter to the editor regarding “association between sarcopenia on residual back pain after percutaneous kyphoplasty for osteoporotic vertebral compression fractures”

article en

Abstract

We commend Chengming Li et al. for examining the link between sarcopenia and residual back pain after PKP. However, their retrospective single‑center study (N = 231) has notable limitations. Sarcopenia was diagnosed solely via SMI at T12 on CT, without functional measures (e.g., grip strength, gait speed), and T12 is not a standard spinal muscle evaluation level, risking diagnostic bias. Pain was assessed only by VAS, lacking detail on characteristics or frequency, hindering mechanistic insight. Causal inference is weak due to unaddressed reverse causality-pre‑operative pain may cause disuse atrophy-and uncontrolled confounders like protein intake, vitamin D, and medications. Methodological transparency is insufficient: missing data handling among 472 initial patients was unspecified, and surgical details (team, experience, cement distribution) were omitted, affecting reproducibility. Finally, proposed mechanisms (biomechanical imbalance, chronic inflammation) rely solely on cited literature without direct validation from study data, such as inflammatory markers or spinal stability assessments.

Journal of Orthopaedic Surgery and ResearchVol. 21(1)
North Sichuan Medical University (CN), Affiliated Hospital of North Sichuan Medical College (CN)
Openalex Percentile: Top 10%
Bone health and osteoporosis research
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